Gastroduodenitis,Aarskog-Scott Syndrome

Nystagmus 7, Congenital, Autosomal Dominant,Nystagmus 3, Congenital, Autosomal Dominant,Congenital Nystagmus,Pathologic Nystagmus,Nystagmus 2, Congenital, Autosomal Dominant,Nystagmus 4, Congenital, Autosomal Dominant

Leukemia,Open-Angle Glaucoma,Glaucoma, Primary Open Angle

Speech Disorder,Epilepsy, Focal, With Speech Disorder And With Or Without Mental Retardation

Locked-In Syndrome,Epidermolysis Bullosa Simplex, Dowling-Meara Type

Atrophic Rhinitis,Giant Axonal Neuropathy,Megaesophagus,Skin Lipoma,Immunodeficiency 62

Gastric Tubular Adenocarcinoma

Atrophic Rhinitis,Moyamoya Angiopathy,Rhabdomyosarcoma

Breast Cancer,Skin Squamous Cell Carcinoma,Oppositional Defiant Disorder

Vaccinia,Schizophrenia 1,Down Syndrome,Autism Spectrum Disorder,Chromosomal Duplication Syndrome

Corneal Dystrophy,Long Qt Syndrome,Breast Cancer,Crouzon Syndrome With Acanthosis Nigricans,Long Qt Syndrome 1

Heart Septal Defect,Heart Disease,Lung Cancer Susceptibility 3,Pulmonary Valve Stenosis,Atrial Heart Septal Defect,Neurofibromatosis-Noonan Syndrome,Neuroma,Hypertrophic Cardiomyopathy,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Costello Syndrome,Joubert Syndrome 3,Neurofibromatosis, Type I,Villonodular Synovitis,Pilocytic Astrocytoma,Fibromatosis,Cryptorchidism, Unilateral Or Bilateral,Skin Granular Cell Tumor,Pseudo-Turner Syndrome,Noonan Syndrome 1,Noonan Syndrome And Noonan-Related Syndrome,Dilated Cardiomyopathy,Aortic Valve Disease 1,Gingival Hypertrophy,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Adenocarcinoma,Neurofibromatosis,Breast Cancer,Patent Foramen Ovale,Colorectal Cancer,Gingival Overgrowth,Pulmonary Valve Disease,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Noonan Syndrome 3,Gingival Disease,Prostate Cancer,Keratosis Pilaris Atrophicans,Noonan Syndrome 4,Prostate Transitional Cell Carcinoma,Fibromatosis, Gingival, 1,Tetralogy Of Fallot,Epilepsy, Familial Temporal Lobe, 8,Patent Ductus Arteriosus 1,Ptosis,Juvenile Myelomonocytic Leukemia,Gingival Fibromatosis,Lung Cancer,Pulmonic Stenosis

Common Variable Immunodeficiency,T-Cell Lymphoblastic Leukemia/Lymphoma,Angioimmunoblastic T-Cell Lymphoma,Leukemia, Acute Myeloid,Burkitt Lymphoma,T-Cell Acute Lymphoblastic Leukemia,Leukocyte Adhesion Deficiency, Type I,Neuropathy, Hereditary Sensory, Type Id,Wiskott-Aldrich Syndrome,Acute Promyelocytic Leukemia,Cd45 Deficiency,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema

Intellectual Developmental Disorder, Autosomal Dominant 44, With Microcephaly,Trio-Related Intellectual Disability,Microcephaly,Clark-Baraitser Syndrome,Deafness, Autosomal Recessive 28,Disease Of Mental Health,Hermansky-Pudlak Syndrome 7,Intellectual Developmental Disorder, Autosomal Dominant 63, With Macrocephaly

Fetal Macrosomia